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1-Butanol, 4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-, benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

321887-73-4

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321887-73-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 321887-73-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,1,8,8 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 321887-73:
(8*3)+(7*2)+(6*1)+(5*8)+(4*8)+(3*7)+(2*7)+(1*3)=154
154 % 10 = 4
So 321887-73-4 is a valid CAS Registry Number.

321887-73-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-((tert-butyldimethylsilyl)oxy)butyl benzoate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:321887-73-4 SDS

321887-73-4Relevant academic research and scientific papers

Ligand-assisted rate acceleration in lanthanum

Hatano, Manabu,Furuya, Yoshiro,Shimmura, Takumi,Moriyama, Katsuhiko,Kamiya, Sho,Maki, Toshikatsu,Ishihara, Kazuaki

supporting information; experimental part, p. 426 - 429 (2011/04/15)

The transesterification of an equimolar mixture of carboxylic esters and primary (1°), secondary (2°), and tertiary (3°) alcohols in hydrocarbon solvents was promoted with high efficiency by a lanthanum(III) complex, which was prepared in situ from lanthanum (III) isopropoxide (1 mol %) and 2-(2-methoxyethoxy)ethanol (2 mol %). The present La(III) catalyst was highly effective for the chemoselective transesterification in the presence of competitive 1°-and 2°-amines. Remarkably, esters were obtained in good to excellent yields as colorless materials without an inconvenient workup procedure.

A novel and efficient method for the silylation of alcohols with methallylsilanes catalyzed by Sc(OTf)3

Suzuki,Watahiki,Oriyama

, p. 8903 - 8906 (2007/10/03)

Reaction of alcohols with methallylsilanes in the presence of a catalytic amount of Sc(OTf)3 provides efficiently the corresponding alkyl silyl ethers. By using microencapsulated (MC) Sc(OTf)3, which can be easily recovered and reused, yields of alkyl silyl ethers are improved and the work-up process after completion of the reaction is considerably simplified. (C) 2000 Elsevier Science Ltd.

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